BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA

    MDR report key: 3934544 · Received July 10, 2014

    Report

    Report Number
    MW5037248
    Event Type
    Injury
    Date Received
    July 10, 2014
    Date of Event
    June 6, 2014
    Report Date
    July 9, 2014
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    MOTHER HAD INJECTIONS OF ROOSTERS COMB INTO KNEES WITH IN THE LAST 6 MONTHS, NOW IN HOSPITAL WITH BRAIN TUMOR AND SPOT ON LUNG. MAY BE LUNG CANCER. MEDICINE EUFLEXXA AND ARTHROCEN WITH ASPIRING INJECTION. DATES OF USE: ONE MONTH. DIAGNOSIS OR REASON FOR USE: IN LIEU OF KNEE REPLACEMENT THERAPY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    402511 EUFLEXXA NONE MOZ

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Hospitalization| L| O| S